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用于制备三元 Fe(1-x)PtRu(x)纳米晶体的简单置换反应,该纳米晶体在甲醇氧化反应中具有优异的催化活性。

Simple replacement reaction for the preparation of ternary Fe(1-x)PtRu(x) nanocrystals with superior catalytic activity in methanol oxidation reaction.

机构信息

Department of Chemistry, National Taiwan Normal University, Taipei 116, Taiwan.

出版信息

J Am Chem Soc. 2012 Jun 20;134(24):10011-20. doi: 10.1021/ja3010754. Epub 2012 Jun 7.

Abstract

The finding of new metal alloyed nanocrystals (NCs) with high catalytic activity and low cost to replace PtRu NCs is a critical step toward the commercialization of fuel cells. In this work, a simple cation replacement reaction was utilized to synthesize a new type of ternary Fe(1-x)PtRu(x) NCs from binary FePt NCs. The detailed structural transformation from binary FePt NCs to ternary Fe(1-x)PtRu(x) NCs was analyzed by X-ray absorption spectroscopy (XAS). Ternary Fe(35)Pt(40)Ru(25), Fe(31)Pt(40)Ru(29), and Fe(17)Pt(40)Ru(43) NCs exhibit superior catalytic ability to withstand CO poisoning in methanol oxidation reaction (MOR) than do binary NCs (FePt and J-M PtRu). Also, the Fe(31)Pt(40)Ru(29) NCs had the highest alloying extent and the lowest onset potential among the ternary NCs. Furthermore, the origin for the superior CO resistance of ternary Fe(1-x)PtRu(x) NCs was investigated by determining the adsorption energy of CO on the NCs' surfaces and the charge transfer from Fe/Ru to Pt using a simulation based on density functional theory. The simulation results suggested that by introducing a new metal into binary PtRu/PtFe NCs, the anti-CO poisoning ability of ternary Fe(1-x)PtRu(x) NCs was greatly enhanced because the bonding of CO-Pt on the NCs' surface was weakened. Overall, our experimental and simulation results have indicated a simple route for the discovery of new metal alloyed catalysts with superior anti-CO poisoning ability and low usage of Pt and Ru for fuel cell applications.

摘要

发现具有高催化活性和低成本的新型金属合金纳米晶(NCs)来替代 PtRu NCs 是燃料电池商业化的关键步骤。在这项工作中,利用简单的阳离子取代反应,从二元 FePt NCs 合成了一种新型三元 Fe(1-x)PtRu(x) NCs。通过 X 射线吸收光谱(XAS)分析了从二元 FePt NCs 到三元 Fe(1-x)PtRu(x) NCs 的详细结构转变。三元 Fe(35)Pt(40)Ru(25)、Fe(31)Pt(40)Ru(29)和 Fe(17)Pt(40)Ru(43) NCs 在甲醇氧化反应(MOR)中表现出比二元 NCs(FePt 和 J-M PtRu)更强的抗 CO 中毒能力。此外,三元 NCs 中,Fe(31)Pt(40)Ru(29) NCs 的合金化程度最高,起始电位最低。此外,通过确定 NCs 表面上 CO 的吸附能以及使用基于密度泛函理论的模拟从 Fe/Ru 到 Pt 的电荷转移,研究了三元 Fe(1-x)PtRu(x) NCs 具有优异 CO 抗性的原因。模拟结果表明,通过向二元 PtRu/PtFe NCs 中引入一种新的金属,可以大大增强三元 Fe(1-x)PtRu(x) NCs 的抗 CO 中毒能力,因为 NCs 表面上 CO-Pt 的键合被削弱。总的来说,我们的实验和模拟结果表明了一种发现具有优异抗 CO 中毒能力和低 Pt 和 Ru 用量的新型金属合金催化剂的简单途径,可用于燃料电池应用。

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